- A Case of Unilateral Retinitis Pigmentosa
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Kim KH, Park YH, Hahn DK
- KMID: 2022646
- J Korean Ophthalmol Soc.
- 1996 Jun;37(6):1090-1094.
Retinitis pigmentosa has been recognized as a symmetrical, bilateral, hereditary, tapetoretinal degeneration with night blindness, visual field loss, and abnormal ERG. Unilateral retinitis pigmentosa is a rather rare disease. Pedraglia... -
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- A Case of Retinitis Pigmentosa without Pigment
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Baek JH, Lee CY, Kim JH, Ma JK
- KMID: 1948773
- J Korean Ophthalmol Soc.
- 1981 Jun;22(2):457-462.
Retinitis pigmentosa without pigment is a varient of retinitis pigmentosa which is a hereditory disorder. It is characterized by decreased visual acuity, night blindness and contraction of visual field in... -
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- Strategies for Mutation Discovery in Retinitis Pigmentosa: Transition to the Next Generation
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Yoon CK, Yu HG
- KMID: 2055573
- J Genet Med.
- 2013 Jun;10(1):13-19.
- doi: 10.5734/JGM.2013.10.1.13
Retinitis pigmentosa (RP) is the most common hereditary retinal disorder and is characterized by progressive retinal degeneration and decline in vision. RP comprises a heterogeneous group of disorders caused by... -
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- Pars Plana Vitrectomy for Vitreous Hemorrhage in Coats-Type Retinitis Pigmentosa
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Lee JH, Kim TK, Kim SY, Lee YC, Lee MY
- KMID: 2212806
- J Korean Ophthalmol Soc.
- 2016 Apr;57(4):677-681.
- doi: 10.3341/jkos.2016.57.4.677
PURPOSE: For vitreous hemorrhage induced by coats-types retinitis pigmentosa, we report a case treated with pars plana vitrectomy and endolaser photocoagulation. CASE SUMMARY: A 24-year-old male who was diagnosed with retinitis... -
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- Electrophysiologic Finding of Retinitis Pigmentosa Inversus and Differential Diagnosis from Peripapillary Choroidal Dystrophy
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Han KH, Kim JW
- KMID: 2108037
- J Korean Ophthalmol Soc.
- 1996 Feb;37(2):275-283.
The authors found 3 cases of retinitis pigmentosa inversus who had characteristics that age of onset is between fifth and sixth decade, retinal lesion was seen around the optic disc... -
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- A Case of Pigmented Paravenous Retino-Choroidal Atrophy and Retinitis Pigmentosa
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Cho HT, Kim SY, Kim SH
- KMID: 1968205
- J Korean Ophthalmol Soc.
- 1991 Oct;32(10):903-909.
Pigmented paravenous retinochoroidal atrophy(PPRCA) is an uncommon disease that was first reported in 1937 by T.H.Brown. The diagnosis was based on the distinctive fundus appearance of bone corpuscular pigment accumulation,... -
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- A Case of Type 1 Ushers Syndrome with Bilateral Cataract
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Lee SJ, Lee JH, Choi YJ, Kim JW
- KMID: 2205301
- J Korean Ophthalmol Soc.
- 1998 Apr;39(4):784-789.
Ushers syndrome is an autosomal recessively inherited entity which is characterized by a retinitis pigmentosa and congenital sensorineural hearing loss. This syndrome represents different clinical features according to its subtypes.... -
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- A Case of Laurence-Moon-Biedl Syndrome
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Jeon PK, Ohn YH, Park JO, Kim CH
- KMID: 1601081
- Korean J Pediatr Gastroenterol Nutr.
- 2003 Mar;6(1):78-83.
Laurence-Moon-Biedl syndrome is an autosomal recessive disorder characterized by obesity, hypogenitalism, polydactyly, mental retardation and retinitis pigmentosa. Occasionally, this syndrome is accompanied by renal anomaly, nystagmus, cataract, syndactyly, microcephaly, oxycephaly... -
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- A Case of Laurence-Moon-Biedl Syndrome
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Kim SD, Kim YK, Kim JD
- KMID: 1949261
- J Korean Ophthalmol Soc.
- 1989 Aug;30(4):671-674.
Laurence-Moon-Biedl syndrome is a rare and autosomal recessive disorder characterized by obesity, hypogenitalism, polydactylism, mental retardation and retinitis pigmentosa. Occasionally, this syndrome is accompanied by nystagmus, cataract, syndactylism, microcephaly, oxycephaly... -
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- Retinitis Pigmentosa Associated with Bardet-Biedl Syndrome with BBS9 Gene Mutation in a Korean Patient
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Kim YH, Joo KS, Seong MW, Park SS, Woo SJ
- KMID: 2469294
- Korean J Ophthalmol.
- 2020 Feb;34(1):94-95.
- doi: 10.3341/kjo.2019.0083
No abstract available. -
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- A Case of Usher Syndrome
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Kim LS, Han CS, O YJ, Kim DW, Hur JW
- KMID: 2074447
- Korean J Otolaryngol-Head Neck Surg.
- 2001 Oct;44(10):1112-1115.
The usher syndrome (US) is an autosomal recessive disorder characterized by congenital bilateral sensorineural hearing loss and progressive visual loss secondary to retinitis pigmentosa. It is the most common cause... -
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- Identification of Compound Heterozygous EYS Variants in a Korean Patient with Retinitis Pigmentosa
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Kim HT, Jang JH, Kang K, Ki CS, Chung H
- KMID: 2407565
- Lab Med Online.
- 2018 Apr;8(2):66-70.
- doi: 10.3343/lmo.2018.8.2.66
No abstract available. -
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- Clinical Survey of 43 Cases of Pigmentary Degeneration of the Retina Including 3 Cases of Laurens-Moon-Biedl Syndrome
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Kim SM, Yoon BJ
- KMID: 1948651
- J Korean Ophthalmol Soc.
- 1964 Nov;5(2):55-62.
Summary: Forty three cases of the pigmentary degeneration of the retina (P.D.R.) visited N.M.C. from Nov. 1958 to Sept. 1964 were analysed clinically in regard to various factors which were... -
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- Two Cases Usher's Syndrom in two Brothers
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Kim KH, Lee SJ, Lee HK
- KMID: 2107829
- J Korean Ophthalmol Soc.
- 1995 Jan;36(1):153-159.
Usher's syndrome is an autosomal recessively inherited trait that characterized by a congenital nonprogressive sensorineural hearing impairment and progressive night-blinding disorder, retinitis pigmentosa, with cataract, psych psis, speech disorder, mental... -
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- Retinitis Pigmentosa Complicated by Vitreous Hemorrhage in a Young Patient: A Case Report
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Chung IY, Huh HD, Kim SJ, Han YS, Seo SW, Park JM
- KMID: 2338388
- J Korean Ophthalmol Soc.
- 2013 Aug;54(8):1293-1297.
PURPOSE: To report a case of a young male patient with retinitis pigmentosa (RP) accompanied by vitritis and neovascularization of the optic disk in both eyes who underwent unilateral vitrectomy... -
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- Atypical Radiologic Manifestation of NARP Mimicking MELAS: a Case Report
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Lee Y, Lee D, Hwang H
- KMID: 2415891
- Investig Magn Reson Imaging.
- 2018 Jun;22(2):119-122.
- doi: 10.13104/imri.2018.22.2.119
Neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome is a rare maternally inherited mitochondrial disorder. Radiologic findings in NARP syndrome are varied; they include cerebral and cerebellar atrophy, basal ganglia... -
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- Bilateral Spontaneous Dislocation of Intraocular Lenses within the Capsular Bag in a Retinitis Pigmentosa Patient
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Lee HJ, Min SH, Kim TY
- KMID: 1115784
- Korean J Ophthalmol.
- 2004 Jun;18(1):52-57.
- doi: 10.3341/kjo.2004.18.1.52
A 45-year-old man with retinitis pigmentosa (RP), who had undergone uneventful extracapsular cataract extraction (ECCE) in his right eye eight years previously, and phacoemulsification in his left eye six years... -
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- Unilateral Retinitis Pigmentosa: A Case Series and Literature Review
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Yoo SH, Sun HJ, Lee SJ, Ohn YH
- KMID: 2215706
- J Korean Ophthalmol Soc.
- 2015 Apr;56(4):559-566.
- doi: 10.3341/jkos.2015.56.4.559
PURPOSE: We report 4 cases of unilateral retinitis pigmentosa (URP) with a literature review. METHODS: A retrospective, observational case series of 4 URP patients with no signs of bilateral involvement during... -
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- Bilateral Spontaneous Anterior Lens Dislocation in a Retinitis Pigmentosa Patient
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Kwon YA, Bae SH, Sohn YH
- KMID: 1101916
- Korean J Ophthalmol.
- 2007 Jun;21(2):124-126.
- doi: 10.3341/kjo.2007.21.2.124
PURPOSE: To report a case of bilateral spontaneous anterior lens dislocation associated with retinitis pigmentosa (RP). METHODS: A 45-year-old male with RP presented with elevated intraocular pressure (IOP)... -
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- Chlorogenic Acid Supplementation Improves Multifocal Electroretinography in Patients with Retinitis Pigmentosa
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Shin JY, Yu HG
- KMID: 1796924
- J Korean Med Sci.
- 2014 Jan;29(1):117-121.
- doi: 10.3346/jkms.2014.29.1.117
To evaluate the effect of chlorogenic acid supplementation in patients with retinitis pigmentosa, we evaluated objective change in visual function with multifocal electroretinography, along with visual acuity, visual field, standard... -
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